Special

HsaINT0049165 @ hg19

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 1 [Source:HGNC Symbol;Acc:2940]
Coordinates
chr3:52400473-52400903:+
Coord C1 exon
chr3:52400473-52400564
Coord A exon
chr3:52400565-52400748
Coord C2 exon
chr3:52400749-52400903
Length
184 bp
Sequences
Splice sites
5' ss Seq
ACTGTAAGC
5' ss Score
4.95
3' ss Seq
TCAGGCGGTCCGTCTCCCAGTGT
3' ss Score
5.8
Exon sequences
Seq C1 exon
GCTTCCTGACAAAGTGCATCCAGCTCTACGAGACCACGGTGGTACGACACGGCCTCATGCTCGTCGGGCCCACAGGCTCCGGCAAGAGTACT
Seq A exon
GTAAGCAGAGCCAAGCTTGGCAGCCAGTGTCCGGATAGTGGGCCTGTAGGGGGGTGCAGCTTCAACAGGGGTTGGCCTCCATTTGTGCCCCTTGGCATAGAATACCCCTCCCCCTCCCCTTGGCCCCCAGCCCACTCTAGCCCTGCTCTCTGGGAGCCTCACTCTCAGGCGGTCCGTCTCCCAG
Seq C2 exon
TGTTACAGAGTCCTGGCAGCTGCCATGACGTCACTGAAAGGGCAGCCATCCATCAGTGGTGGCATGTACGAGGCTGTCAACTACTACGTGCTCAACCCCAAGTCCATCACGATGGGCCAGCTGTACGGGGAGTTTGACCTCCTCACCCATGAGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114841-DNAH1:NM_015512:35
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF077289=AAA_5=PU(8.8=41.9)
A:
NA
C2:
PF077289=AAA_5=FE(34.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCTGACAAAGTGCATCCAGC
R:
CTCATGGGTGAGGAGGTCAAAC
Band lengths:
242-426
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development